Quality & Compliance
Regulated-grade processes, traceable supply chains and audit-ready documentation — built to meet pharma, food and EU clean-label expectations.
Our Quality Pillars
We operate under documented ISO systems with a combination of in-house and accredited third-party testing (GC / GC-MS) and C-14 compliance readiness. COAs are issued per batch and provided to qualified buyers.
Quality Workflow (summary)
Analytical & Spec Highlights
| Parameter | Mansa Nutri — Natural Citral | Typical Test |
|---|---|---|
| Purity | ≥85% (avg. ~87.1%) | GC area % |
| Solvent Residue | Not detected / solvent-free | GC / Residue analysis |
| Residual Pesticides | Validated below method LOQ | LC-MS/MS |
| Microbial | Compliant with pharma handling | Plate counts / specific tests |
| Radiocarbon (C-14) | ~100% pMC (consistent with plant origin; compliance ready) | AMS / Radiocarbon test |
Verified Documentation & Testing
Batch COA
Full COA available on request — includes GC summary, impurities, and packaging details. Provided per batch to qualified buyers.
GC / GC-MS Reports
GC/GC-MS chromatograms and method details are shared with qualified buyers; testing performed in-house and with accredited third-party labs as appropriate.
C-14 / Origin Validation
Radiocarbon tests are supported per order — Mansa Nutri material is C-14 compliance ready and can be validated through accredited AMS providers as requested.
Supply Assurance & Packaging
MOQ, lead time and pharma-grade packaging (20 kg / 200 kg drums) are confirmed at enquiry. Export documentation, handling protocols and required QA paperwork are provided for regulated markets.
Frequently Asked Questions
Last updated: 2025. For technical discussions and specific test requests, contact our quality team via the contact page or the Request COA link above.
